Process for processing elastomeric compositions

ABSTRACT

A process is provided for producing elastomeric compositions by forming a mixture of polymeric material, a reinforcing agent, a processing aid and a vulcanizing agent. The process of the invention is continuous and includes the repeated, sequential steps of admixing the polymeric material along a first mixing zone defined by a space wherein the gross energy applied induces a first operating temperature range. The mixture of the first zone is continuously passed into and through a second mixing zone while adding and admixing the reinforcement agent and processing aid therewith, the second mixing zone being defined by a space wherein the gross energy applied induces a second operating temperature range. The mixture of the second zone is then continuously passed into and through a third mixing zone while adding and admixing the vulcanizing agent therewith, the third mixing zone being defined by a space wherein the gross energy applied induces a third operating temperature range. The mixture of said third zone is the continuously passed into and through a delivery zone to extrude the mixture in the form of the elastomeric composition, with the second and third operating temperature ranges being lower than the first operating temperature range.

BACKGROUND OF THE INVENTION

1. Field of the Invention

The present invention relates generally to the production of elastomericcompositions and, more particularly, to the mixing and production ofrubber. Specifically, the present invention relates to an improvedprocess for the continuous mixing and production of elastomericcompositions.

2. Description of the Prior Art

The conversion of elastomeric compositions, and in particularelastomeric polymers such as rubber, into commercially significantmaterials has been a focal point of the rubber industry throughout itshistory. The earliest commercial process was largely based on a mixingprocess utilizing two-roll mills to modify the basic polymer'scharacteristics by adjusting the viscosity of the polymer as well as byincorporating enhancing ingredients such as reinforcing agents,modifying oils and curatives. Over the years, a wide variety of mixingprocesses and devices have evolved in the rubber industry. A thoroughtreatment of such development is set forth in an article entitled,"Development of Internal-Mixer Technology for the Rubber Industry" byJames L. White, Rubber Chemistry and Technology, Volume 65, page 528,the contents of which are specifically incorporated herein by reference.

The elastomer mixing process is basically defined as combining theingredients specified in an elastomeric recipe, on some schedule ofaddition, and under some regime of mastications for a certain period oftime and/or temperature. Rubber elastomer mixing technology is focusedprincipally upon controlling five principal features of the mixingprocess independent of the recipe specifics. One feature of concern isthe uniform distribution of raw materials of the elastomer recipethroughout a single unit mass or volume. The second feature involvesdispersive mixing which focuses on the intimate association of theelastomer ingredients in a physical sense, typically at a molecularlevel, which influence the mechanical characteristics of the finalcomposition. The third feature involves viscosity modification while thefourth feature is concerned with chemical reactions of the ingredients.The final feature involves, of course, economic considerations whichcontrol capital utilization and manufacturing costs. These five factorsare interrelated, often inversely, and they are sensitive to rate,volume, power, time and temperature limitations.

With the advent of the Banbury mixer, which is described in theabove-referenced article, and its commercial adoption, the rubberindustry was able to substantially increase uniformity of the processand productivity of manufacturing elastomeric compositions. TheBanbury-type intensive mixer, and its many modifications and adaptationsas indicated, still remains the primary processing device and process inthe rubber industry throughout the world today.

While the Banbury-type intensive mixing process has been adequate, ithas certain limitations. Principal among such limitations is the batchor unit production nature of the process. This process requires aminimum of several passes through the Banbury mixer in order toincorporate all ingredients of an elastomeric composition since theBanbury is a batch-type process. This feature is the principal source ofvariation in characteristics of the final mixed elastomeric stock.Variation in the weights of individual ingredients, the order ofaddition, timing of addition and discharge, initial temperature of theraw materials and ingredients, and the process environment allcontribute to batch-to-batch variation. Even with recent improvements tothe Banbury-type process which include automatic weighing systems andcomputer controlled batch cycles, batch-to-batch variation controlremains barely adequate requiring sophisticated protocols for batchblending in subsequent processes.

Another limitation of the Banbury-type process involves the volumetricdynamics of the large working volume of this process. Economic necessitydictates that Banbury-type intensive mixers be scaled to the largestsize appropriate to the manufacturing operation. As a result, effectivevolumetric mixing of a high viscosity mass becomes even more difficult.Concurrent with limitations in volumetric mixing efficiency arethermodynamic control problems due to the marginal, and declining,surface area to mass ratio of increasing volumes within the Banburymixer.

In order to avoid the aforementioned problems associated with batchmixing processes such as utilized by the Banbury mixer, the rubberindustry has attempted to devise continuous mixing systems utilizing avariety of extrusion-type devices. The driving incentives for devisingsuch continuing processes include improved uniformity throughsteady-state processing, better thermal management resulting fromimproved surface-to-mass ratios, and developing opportunities for highlyautomated operations. A variety of processes and devices have beencreated in attempts to incorporate technical rubber and elastomericmixing features with extrusion processing systems utilized in otherindustries. Such extrusion-type devices have been used in the plasticsand baking industries for some time. An example of this is illustratedin U.S. Pat. No. 5,158,725. While such devices and processes haveenjoyed significant applications in the rapid expansion of thermoplasticpolymer processing, none have been widely successful for adaptation bythe rubber industry.

A combination of diverse forces have inhibited, up to now, the adoptionof continuous extrusion-based processes by the rubber industry.Principal among these forces has been the consistent inability ofextrusion-based processes to demonstrate improved uniformity ateconomically productive rates while maintaining the desiredcharacteristics of the final elastomeric composition. Other factors haveincluded sparse availability of suitable polymer forms, barely adequatemass flow metering systems, and continued inability to control thethermodynamics of the process. Such a lack of thermodynamic control hasresulted in unacceptable blending and mixing and in premature curing ofelastomers within the extrusion devices. The present invention overcomesthe aforementioned disadvantages of batch-type Banbury mixers, as wellas overcomes the disadvantages of prior continuous processes such as thecontrol of process thermodynamics and uniform elastomer mixing.

SUMMARY OF THE INVENTION

Accordingly, it is an object of the present invention to provide animproved process for the mixing and production of elastomericcompositions and in particular rubber.

It is another object of the present invention to provide a continuousprocess utilizing extrusion-type devices for the mixing and productionof elastomeric compositions.

It is a further object of the present invention to provide a continuousrubber mixing process which inherently controls the thermodynamics ofthe process to enhance polymer mixing and to prevent polymer degradationand premature curing.

Another object of the present invention is to provide a continuousprocess for the mixing and production of elastomers which assuresuniform distribution of the components thereof.

To achieve the foregoing and other objects and advantages, and inaccordance with the purposes of the present invention, as embodied andbroadly described herein, a process for producing elastomericcompositions is provided by forming a mixture of polymeric material, areinforcing agent, a processing aid and a vulcanizing agent. The processis continuous and includes the repeated sequential steps of admixing thepolymeric material along a first mixing zone defined by a space whereinthe gross energy applied induces a first operating temperature range.The mixture of the first mixing zone is continuously passed into andthrough a second mixing zone while adding and admixing the reinforcingagent and processing aid therewith, the second mixing zone being definedby a space wherein the gross energy applied induces a second operatingtemperature range. The mixture of the second zone is then continuouslypassed into and through a third mixing zone while adding and admixingthe vulcanizing agent, the third mixing zone being defined by a spacewherein the gross energy applied induces a third operating temperaturerange. This mixture from the third zone is then continuously passed intoand through a delivery zone to extrude the mixture in the form of anelastomeric composition, the second and third operating temperatureranges being lower than the first operating temperature range.

BRIEF DESCRIPTION OF THE DRAWINGS

The accompanying drawings, which are incorporated in and form a part ofthe specification, illustrate preferred embodiments of the presentinvention, and together with a description, serve to explain theprinciples of the invention. In the drawings:

FIG. 1 is a flow diagram illustrating the sequential staging of theprocess of the present invention; and

FIG. 2 is a schematic cross section of a typical twin-screw extruderadapted to incorporate the process of the present invention.

DESCRIPTION OF THE PREFERRED EMBODIMENTS

The process of the present invention involves the continuous uniform netflow of elastomers including rubbers, rubber/thermoplastic polymermixtures, and the like, with reinforcing agents including fillers,processing aids such as oils, waxes and the like, and curativesappropriate to the application through a system of at least three andpreferably four discrete zones of mixing and controlled materialaddition. In each of these mixing zones, the shear rate, shear stress,energy flux and temperature are interrelated and individuallycontrollable in order to produce an elastomeric material of improveduniformity at economically productive rates. By carefully controllingthese variables in each zone, the energy balance and equilibrium can bemaintained to permit the process to run at equilibrium or at a steadystate without external temperature control mechanisms which are notadequate due to slow heat transfer of elastomers.

The composition components may be those typical of any type ofelastomeric composition recipe. The rubber elastomers may include, butare not limited to, natural rubber, cis-polyisoprene, styrenebutadiene,acrylonitrile-butadiene, polychloroprene rubber,poly-(ethylene-propylene diene monomer), cis-polybutadiene,polyacrylate, poly-isobutylene, poly-chloroisobutylene, and siliconerubbers. Typical thermoplastic polymers may include, but are not limitedto, polyvinyl chloride, polyethylene, polypropylene, polyamide,polyester, polyether, polyethylene-acrylate, flouropolymers, and ionomerpolymers.

The reinforcing agents may include one or more of, but are not limitedto, carbon black, fumed and precipitated silica, siliane treated clays,and short fibers of reinforcing materials. The reinforcement agents mayalso include fillers such as calcium carbonate, talc, kaolin clays,silicas and petroleum coke. Processing aids may include oils and waxes.Other added components may also include anti-oxidants/ozonants, adhesionpromoters, fire retardants, foaming agents, compatibilizers andcolorants. The oils, both plastizing and extending, may be eitherpetroleum or pthalate-ester based as appropriate. Finally, curativesuseful with the present invention may be of any desired selection butare preferably, although not exclusively, amine catalyzed sulphursystems, other sulfur containing organic compounds, metal oxides andperoxides.

While certain specific examples will be discussed with respect to theprocess of the present invention, it should be understood that thepresent invention is applicable to a wide variety of elastomericcompositions, recipes and components thereof and may include reinforcedelastomers as well as elastomeric alloys.

Referring now to FIG. 1, a flow diagram 10 is illustrated therein. Inthis flow diagram 10, the process of the invention is divided into aplurality of mixing zones including a first mixing zone 12, a secondmixing zone 14, a third mixing zone 16, which is optional, a fourthmixing zone 18 and a fifth zone 20 which is, in preferred form, adelivery or extruding zone as described below. The composition mixtureis processed and moved through zones 12-20 in the direction indicated bythe arrow 22. The polymer mixture 24 is added at the beginning of thefirst mixture zone 12, and the reinforcing agents 26 and the processingaids 28 are preferably separately and sequentially added as indicated atthe beginning and mid-portion of the second mixing zone 14. An optionalmixing zone 16 may be included wherein the same or additionalreinforcing agents 30 and processing aids 32 are separately added to thecomposition flow 22. Finally, the curatives or vulcanizing agents 34 areadded at the beginning of the mixing zone 18 to complete the additionand admixing of the various components of the elastometric composition.The mixture flow 22 is then directed through the delivery zone 20wherein the mixture flow is extruded into the form of the finalelastomer composition through some sort of die slot or the like.

Referring now to FIG. 2, the process of the present invention, inpreferred form, is accomplished by continuously metering, individuallyand preferably gravimetrically by weight loss feeders, particulatedmaterials and/or liquids as described above in the proportion prescribedby the particular application formula or recipe, to an extrusion device36 capable of applying about 0.08-0.23 KW-Hrs/Kg shear energy on acontinuous basis. For the purposes of the process of the presentinvention, any type of device 36, including stacked Banburys, which willincorporate the process of the invention may be utilized. The genericextruder device 36 as disclosed in FIG. 2, includes a barrel 38 having apair of central cylinders 40 and a pair of extrusion screws 42positioned within the cylinders 40 (with only one cylinder 40 and screw42 being illustrated). As each screw 42 rotates within the barrel 38,elastomeric materials pass through the cylinder 40 from the first zoneindicated at 12 to the fifth zone indicated at 20. A feed device 43 isprovided to feed polymeric material 24 into the first zone 12, whilefeed devices 44 and 46 are provided to meter, respectively, reinforcingagents 26 and processing aids 28 into the second mixing zone 14.Metering or feed elements 48, 50 are, likewise, utilized to deliver thesecond set of reinforcing materials 30 and processing aids 32 into theoptional third mixing zone 16. Finally, a metering member 52 is providedto deliver the vulcanization or curing materials 34 into the fourthmixing zone 18.

In preferred form utilizing a twin-screw extruder, the componentparticulate materials must have particle size distributions consistentwith the clearances between the rotating screw element 42 and thestationery walls of the cavity 40 within the barrel 38. The particlesize must be sufficiently small to be distributed quickly and completelyinto the mass of material being mixed. However, finely ground materialsare unnecessary. Polymers 24, in particular, do not require grinding tofine powders and can be chopped to a distributional median of about 80%of the clearance between the screw 42 and the wall of the cylinder 40 atthe point of addition 43.

With respect to a suitable distribution of the physical dimensions ofparticle sizes, a suitable distribution based on weight of particle sizehas been found to range from 1-90% of the maximum radial distancebetween the rotating member 42 and the stationery surface of the cavity40. The mean value, based on weight, preferably ranges from 65-75% ofthe free radial distance.

Typical examples of extrusion devices include intermeshing co-rotatingand counter-rotating twin-screw extruders and certain other multiplescrew masticating extruders. Nominal shear rates should preferably be inthe range of 40-120 sec⁻¹ with localized shear rates reachingsubstantially higher levels such as 1500 sec⁻¹. A preferredconfiguration illustrated at 36 is a single intermeshing co-rotatingtwin screw extruder having a length to diameter ratio (L:D) in the rangeof 30-55 and more preferably 50-55. However, other device configurationsare contemplated as useful with the process of the present invention,including multiple devices arranged in a cascaded fashion with thematerial passing continuously from one device to the next. In allinstances of device configuration, however, provision is made for atleast four separate material addition ports 43, 44, 46 and 52, asindicated above, to provide for incremental addition of theabove-referenced materials in the specific order provided: polymers 24,reinforcing agents and/or fillers 26, processing aids and/or oils 28,and vulcanization agents 34. Provision may be required, depending uponthe characteristics of the formulation being mixed, for up to fouradditional material ports. In the illustrated preferred embodiment, twoadditional material ports 48 and 50 are provided for introducing asecond grouping or set of reinforcing agents 30 and processing aids 32.

It is strongly preferred, though not required, that the internal volumeof the mixing device 36 be incrementally increased at each materialaddition port in proportion to the volume of material introduced at eachport so as to maintain a substantially constant mixing volume fillfactor within the cavity 40. Fill factors may vary in the range of10-90% of the effective volume of the device to accommodate specificrequirements of temperature, viscosity, dispersion and productionthroughput. More preferably, the fill factor volume is in the range10-30%. Moveover, the rotating members of the mixing extruder maypreferably be composed of a variable combination of conveying elementsand semi-conveying elements which make up the screw 42 and which impartdistribute mixing and high shear stress.

Referring now to both FIGS. 1 and 2, the overall process may bedescribed in the following manner. The polymers 24 are introduced intothe process in the first zone 12 by means of individually metered,continuous mass flow streams through the feeder 43 in proportionsappropriate to the desired recipe and at the desired production rate.Certain other chemical modifiers such as zinc oxide, anti-oxidants, andthe like may also be introduced into this first mixing zone 12 alongwith the principal polymers. Anti-oxidants will protect the polymerswhen subjected to higher temperature. However, in the preferredembodiment no reinforcing agents nor processing aids are to beintroduced in this first zone 12.

The combined materials introduced at the beginning of the first zone 12are then subjected to mixing and shearing stresses at programed shearrates for a controlled amount of time resulting in thorough blending ofthe mixture as well as an increase in temperature and reduction ofviscosity. These details are illustrated in Table I. It was discoveredthat by increasing the temperature due to high shear rates and othervariables as indicated herein in the first mixing zone 12, the viscositycould be substantially reduced thereby making the remainder of themixing process and in particular the admixing of the reinforcing agentssuch as carbon black much easier.

                                      TABLE I                                     __________________________________________________________________________                                     16             20                                         FIG. 1                                                                              12     14     ZONE 3  18     DIE                                        UNITS ZONE 1 ZONE 2 (COND)  ZONE 4 ADAPTER                                                                              OVERALL                __________________________________________________________________________    Standard Mass Flow Rate.sup.a                                                              kg/s × m.sup.3                                                                200-900                                                                              425-1800                                                                             515-2100                                                                              525-2150                                                                             NA     525-2150               Standard Volumetric Flow                                                                   m.sup.3 /s × m.sup.3                                                          0.23-0.95                                                                            0.35-1.60                                                                            0.35-1.65                                                                             0.38-1.70                                                                            NA     0.38-1.70              Rate.sup.b                                                                    Exit Temperature                                                                           °C.                                                                          130-220                                                                              110-160                                                                              85-130  115-150                                                                              120-160                                                                              NA                     Gross Energy Applied.sup.c                                                                 J/kg  5.4 × 10.sup.5 -                                                               4.3 × 10.sup.4 -                                                               3.6 × 10.sup.4 -                                                                3.6 × 10.sup.4 -                                                               3.0 × 10.sup.3                                                                 2.9 ×                                                                   10.sup.5 -                                1.1 × 10.sup.4                                                                 7.2 × 10.sup.4                                                                 1.1 × 10.sup.5                                                                  1.1 × 10.sup.5                                                                 4.0 × 10.sup.3                                                                 6.5 ×                                                                   10.sup.5               Net Energy Absorbed.sup.d                                                                  J/kg  -1.8 × 10.sup.5 -                                                              -3.6 × 10.sup.4 -                                                              -3.6 × 10.sup.3 -                                                               -1.8 × 10.sup.4 -                                                              -1.8 × 10.sup.3                                                                -1.1 ×                                                                  10.sup.5 -                                -2.9 × 10.sup.5                                                                -5.4 × 10.sup.4                                                                -2.9 × 10.sup.4                                                                 -6.2 × 10.sup.4                                                                -3.6 × 10.sup.3                                                                -1.8 ×                                                                  10.sup.5               Energy Loss.sup.e                                                                          J/kg  -4.7 × 10.sup.5 -                                                              -3.6 × 10.sup.4 -                                                              -3.6 × 10.sup.3 -                                                               -3.6 × 10.sup.4 -                                                              0.0-   -2.2 ×                                                                  10.sup.5 -                                -6.8 × 10.sup.5                                                                -7.2 × 10.sup.4                                                                -3.6 × 10.sup.4                                                                 -8.0 × 10.sup.4                                                                -3.2 × 10.sup.3                                                                -3.6 ×                                                                  10.sup.5               Minimum Residence Time                                                                     sec   25-50  6-15   6-15    7-20   10-35  54-135                 Median Residence Time                                                                      sec   50-70  10-20  10-20   10-40  15-40  95-190                 Volume Ratio.sup.f                                                                         %     12-25  15-30  10-25   10-25  NA     NA                     Apparent Shear Stress                                                                      Pa    5.0 × 10.sup.8 -                                                               5.0 × 10.sup.7 -                                                               2.0 × 10.sup.7 -                                                                3.0 × 10.sup.7 -                                                               3.5 - 10.sup.4 -                                                                     NA                                        8.0 × 10.sup.8                                                                 7.0 × 10.sup.7                                                                 1.0 × 10.sup.8                                                                  1.0 × 10.sup.8                                                                 4.5 × 10.sup.4          Apparent Viscosity                                                                         Pa × s                                                                        4.0 × 10.sup.4 -                                                               3.0 × 10.sup.4 -                                                               2.5 × 10.sup.4 -                                                                1.0 × 10.sup.4 -                                                               1.7 × 10.sup.5                                                                 NA                                        8.5 × 10.sup.4                                                                 6.5 × 10.sup.4                                                                 6.0 × 10.sup.4                                                                  2.0 × 10.sup.4                                                                 3.5 × 10.sup.5          Applied Energy Surface Flux.sup.g                                                          J/m.sup.2                                                                           2.1 × 10.sup.4 -                                                               6.6 × 10.sup.4 -                                                               6.6 × 10.sup.4 -                                                                1.0 × 10.sup.5 -                                                               NA     1.2 ×                                                                   10.sup.4 -                                5.0 × 10.sup.4                                                                 1.4 × 10.sup.5                                                                 1.0 ×  10.sup.5                                                                 1.1 × 10.sup.5                                                                        2.2 ×                                                                   10.sup.4               __________________________________________________________________________     .sup.(a) Mass flow rate an kg/hr divided by the radius of the cavity          cubed.                                                                        .sup.(b) Volumetric flow rate in cm.sup.3 /second, divided by the radius      of the cavity cubed.                                                          .sup.(c) Total energy applied to the mixing chamber, not including motor      and gear box losses.                                                          .sup.(d) Total energy absorbed the the material passing through the mixin     chamber.                                                                      .sup.(e) Total energy loss from the process to through the walls of the       mixing cavity. Losses are controlled by the thermal conduction rate of th     material and residence time.                                                  .sup.(f) Percentage of the mixing cavity volume occupied by the material.     .sup.(g) Total energy applied per unit area of the mixing cavity surface.

However, this high shear and temperature can only occur over a shortperiod of time, therefor necessitating rapid movement of the mixturethrough this first zone 12.

The masticated polymer mixture is then continuously passed from thefirst zone 12 into the second zone 14 in which individually metered,temperature controlled, mass flow streams of reinforcing agents 26 andprocessing aids 28 are sequentially introduced into the masticatedpolymer mixture. The compounded volume of the materials introduced intothe second zone 14 should preferably not exceed 90% of the volume of thepolymer mixture flowing from the first zone 12. The resultingpolymer/filler-oil mixture or mass-flow composition is then subjected tomixing and shearing stresses at programed shear rates for a controlledperiod of time in the second zone 14, resulting in complete distributiveand dispersive incorporation of the reinforcement materials andprocessing aids. Temperatures and apparent viscosities are typicallyreduced in the second zone 14 as compared to the first zone 12. Thereinforcement materials are preferably carbon black and may also includemineral fillers, short fibers and small chemicals. Oils and waxes arepreferably introduced as the processing aids.

The admixture which has been passed through the second zone 14 is thencontinuously passed into and through the third optional zone 16 ordirectly into the fourth zone 18. The conditional nature of the optionalthird zone 16 is dependent upon the actual recipe requirement of theelastomeric composition for additional reinforcement agents, fillersand/or oils exceeding the volume limit previously indicated for thesecond zone 14. The third zone 16 is typically the zone in which smallconstituent chemicals such as adhesion promoters, anti-ozonants, coloradditives, fire retardants and the like are preferably introduced to theadmixture. The materials introduced to the third zone 16 are againindividually metered, temperature controlled., mass flow streams. Theresultant mixture is then subjected to mixing and shearing stresses atprogrammed shear rates for controlled periods of time to completelydistribute and disburse the materials added. Material temperatures inthe third zone 16 continue to decline as compared to the second zone 14.Apparent viscosities may increase or decrease depending on the nature ofthe materials introduced to the third zone 16.

The mixture from either the second zone 14 or the third zone 16, ifutilized, is then passed continuously into the fourth zone 18 in whichthe vulcanizing agents 34 are added. The vulcanizing agents may includesmall constituent chemicals, curative agents, and the like, and areadded to the mixture at sufficient pressure to develop the force neededto direct the mixture through the exit orifice of the fourth zone 18 andinto and through the delivery zone 20. The completely formulated andmixed material is then passed into the delivery zone 20 wherein thematerial forming die is placed. An appropriate exit die adapter ispositioned where the density of the mixture is increased, and themixture is then forced through a forming surface appropriate to thedesired application for the elastomeric composition. The elastomericcomposition is then subjected to rapid cooling, typically by spraying orimmersion in a water bath, dried, and then deposited in or on anappropriate storage medium.

The process of the present invention provides for superior dispersionand uniformity of component materials as compared to conventional batchmixing processes due to the sequenced adding of the component portionswhile maintaining control of the magnitude and rate of energyapplication, temperature of the material being mixed, total torque onthe mixing equipment, and maximizing material throughput. The preferredvolume flow rates, exit temperatures at each mixing zone, energyapplied, and the like, are all outlined in Table I. As a result of theinvention, the extruder 36 operates at equilibrium without applicationof any external heating or cooling to the device 36. This is due, inpart, to controlling the temperatures of the components as they areadded during the process, thus acting as heat sinks.

Energy management rate and magnitude of the application of energy to theprocess of the present invention is essential in order to obtain themixing objectives desired while limiting undesirable temperature andtorque buildup. Excess temperature buildup, in the first instance, willinitiate premature vulcanization reactions leading to a condition knownas scorch and scrap material. Secondarily, excessive temperature buildupwill oxidize and depolymerize the polymers resulting in loss of physicalproperties. Excessive torque produces negative economic results byshortening mixing device life and reducing productivity as well ascreating excessive temperature.

The process of the present invention functions, in part, due to theacknowledgment of the characteristically poor thermal conductivity ratesof most rubber compounds typically exhibiting thermal conductivity ratesof only one-tenth of the material used in the construction of the mixingdevice. This fact coupled with the rapid transport rate of the mixturethrough the process of the present invention, that is short exposuretimes, precludes the need for significant use of heat exchange media inorder to reduce excessive energy buildup in the mixture. In normaloperation, the process of the present invention proceeds with a mixingdevice at equilibrium with the environment. The rheological propertiesof any particular elastomeric composition recipe are significantlyimportant in the management of energy in the process of invention. Eachpolymer type and each recipe based on that polymer has a unique responseto the application of shearing energy, yielding unique apparent shearstress and temperature rise. The net energy applied to the mixture ineach mixing zone 12-20 results from the energy input from high intensityshearing within the barrel 38 plus transport energy less the energy lostin the environment through the mixer barrel 38. This is expressed by thefollowing relationship:

    ______________________________________                                         ##STR1##                      (1)                                            Glossary                                                                      ______________________________________                                        τ    Apparent shear stress, Pa                                            γ  Apparent shear rate, s.sup.-1                                        γ.sub.s                                                                          High shear region apparent shear rate, s.sup.-1                      γ.sub.t                                                                          Volume transport apparent shear rate, s.sup.-1                       m        Apparent intrinsic viscosity, Pa · s                        n        Characteristic temperature, °K.                               T        Actual temperature, °K.                                       T.sub.1  Initial temperature, °K.                                      T.sub.2  Final temperature, °K.                                        T.sub.cav                                                                              Cavity surface temperature, °K.                               T.sub.a . . . n                                                                        Initial temperature of discrete materials, °K.                M.sub.a . . . n                                                                        Mass flow rate of discrete materials, Kg · s.sup.-1         M.sub.t  Total mass flow rate, Kg · s.sup.-1                         C.sub.pa . . . n                                                                       Discrete heat capacity, J/Kg/°K.                              E.sub.s  Net shear energy applied to material, J                              E.sub.t  Thermodynamic energy applied, J                                      V.sub.s  Volume in high shear region, m.sup.3                                 V.sub.t  Total volume of material transported, m.sup.3                        A.sub.s  High shear region surface area, m.sup.2                              G.sub.s  High shear region cavity-rotor clearance, m                          λ Thermal conductivity coefficient, J/m.sup.2 /°K.              ______________________________________                                    

The gross energy applied is dependent on the shear rates, the volume ofthe mixture in each shearing region, the ratio of mixture volume to thecavity 40 surface, initial temperatures and residence time. The shearrates, in turn, are dependent in part upon relative surface velocitiesand clearances between the screw 42 and cavity wall 40.

As a result of experimental trials as discussed below, it has beendetermined that high rates of energy input through high shear to meltthe polymers and reduce viscosity need only be applied to the polymermass at the first zone 12, with the remaining constituents present inthe elastomeric composition recipe being either low temperature melting,low viscosity liquids, or solids at all processing temperatures throughthe device 36. The input power required for the total process per unitmass of throughput can be minimized by the early and rapid reduction ofthe polymer viscosity within the first mixing section 12. This is animportant contribution to the economic productivity of the process ofthe invention with finite power capability. It has also been discoveredthat effective mechanical blends of polymers within the first mixingzone 12 is best achieved when their respective viscosities are similarin value. This is most effectively accomplished at very high shearrates, that is greater than 600 sec⁻¹ for brief periods of time. Itshould be noted, however, that care must be practiced with shear rateenergy flux so that shear sensitive polymers are not depolymerized aspreviously explained. The energy required to incorporate solidreinforcement materials, including carbon black, is relatively smallwhen compared to the energy required to render the polymers 24sufficiently fluid to facilitate incorporation of the reinforcementmaterials 26. Finally, maintaining low and constant admixture to cavityvolume ratios typically in the 15-30% range, as previously explained,facilitates relatively uniform energy flux, volumetric blending andresidence time in each mixing zone 12-20.

The energy applied to the admixture in each mixing zone of processingmay also be evaluated thermodynamically by applying a `law of mixtures`approach to the discrete mass flows, heat capacities and temperaturechanges of the separate material flows comprising the admixture in eachzone, as in the following relationship: ##EQU1## In order for theprocess of the invention to be balanced and operate in equilibrium,equation (1)=(2). It is evident from equation (2) that temperaturemanagement in any zone may be readily facilitated by sequential controlof mass flow rates, selection of materials, initial materialtemperatures and timing of addition of the various constituentsintroduced to each zone, independent of the thermal status of the mixingdevice. The high energy flux into the polymer in the first zone 12 andresulting increase in temperature, is promptly and effectivelytransferred to the mass of carbon black and oil introduced in the secondzone 14. The result is a rapid progression to equilibrium temperaturewhich is both safe and suitable for further processing.

As previously indicated, the process of the present invention provides auniquely different situation from traditional batch mixing processes inthat there is, at any productivity rate, a static working volume ofmaterial in the batch process which maintains static mixing dynamics andenergy flux. The process of the present invention, however, requiressequential additions which Change the working volume of the material,with ratios from the initial polymer addition to the finally finishedelastomeric composition of 1:2 to 1:3.5. Thus, as previously indicated,the volume of the cavity 40 within each of the mixing zones 12-20 ispreferably increased from zone 12 to 20, preferably in accordance withthe particular ratio range just stated.

EXAMPLE I

The typical formulation of the process of the present invention isdescribed as follows:

                  TABLE II                                                        ______________________________________                                        MATERIAL      WEIGHT PERCENT                                                  ______________________________________                                        Polymer A     20.3                                                            Polymer B     10.1                                                            Carbon Black  33.4                                                            Mineral Filler                                                                              10.5                                                            Processing Oil                                                                              21.2                                                            Zinc Oxide    1.5                                                             Stearic Acid  0.5                                                             Anti-oxidant  0.6                                                             Accelerator A 1.1                                                             Accelerator B 0.6                                                             Sulfur        0.2                                                             ______________________________________                                    

Utilizing this typical formulation, polymer materials 24 added at port43 would include polymer A, polymer B, zinc oxide, and anti-oxidant. Thereinforcement materials 26 added at the port 44 would includeapproximately two-thirds of the carbon black and stearic acid. Theprocessing aids added at the port 46 would preferably include one-halfof the processing oil. In this instance, of course, the third optionalzone 16 is utilized and the materials added at the port 46 would includethe remaining one-third of the carbon black and the mineral fillers,while the remaining one-half of the processing oils will be added at theport 50. Finally, the vulcanizing agents 34 added at the port 52 wouldinclude the accelerator A, accelerator B and sulfur.

In this particular instance, utilizing a preferred intermeshingco-rotating twin screw extruder, mass flow restricter mechanisms wouldpreferably be utilized at the exit of the first mixing zone 12 to assurecomplete viscosity reduction of the elastomer fraction prior to thefirst introduction of the reinforcement materials 26 at the beginning ofthe second mixing zone 14 as well as to regulate and control mass flowof polymer melt relative to the reinforcement material, therebymaintaining correct proportional portions. In each of the followingmixing sections 14-18, the extruder screw 42 is preferably utilized toregulate mass flow and internal metering within the device 36. Controlof temperature, and incremental mix viscosity, within the mixing processof the present invention is vital to control the degree of materialdispersion and the final mixed properties of the elastomericcomposition.

Viscosity may be controlled by a variety of dynamic methodssimultaneously and include adjusting the volumetric fill factor, therotational velocity of the screw 42, the rotational element-to-fixedwall clearances, the order of material addition, the material additiontemperature, the mass flow restriction, and the heat exchange media (ifany) circulated within the device 36. By monitoring temperature andpressure at the exit of each incremental mixing section as indicated inTable I, incremental and/or final viscosities may be measured in realtime and controlled. With the assistance of computerized analysis andcontrol, the mixing process of the invention may be dynamicallycontrolled within a very narrow and consistent control span. Asindicated, residence time within the device 36 is important, and ispreferably 1.2-1.8 minutes from the introduction at the beginning of thefirst mixing zone 12 to the extrusion of the elastomer at the end of thedelivery zone 20.

EXAMPLE II

A number of experimental trials were conducted utilizing five differentelastomeric composition recipes and several different processparameters. The five different recipes are detailed in Table III, andare used merely as examples for the process. The specific selectedcompounds such as the carbon black, pigments, anti-oxidants,accelerators, and the like, are unimportant except that they remain thesame in each recipe throughout all of the different process tests.

                                      TABLE III                                   __________________________________________________________________________             RECIPE 1                                                                            RECIPE 2                                                                            RECIPE 3                                                                            RECIPE 4                                                                            RECIPE 5                                     MATERIAL 100 RHC                                                                             100 RHC                                                                             100 RHC                                                                             100 RHC                                                                             100 RHC                                      __________________________________________________________________________    EPDM A   86.21                                                                EPDM B         15.00 19.35                                                    EPDM C   13.79                                                                EPDM E         85.00 80.65                                                    NBR A                            100.00                                       NBR B                      24.60                                              SBR A                      103.70                                             PVC A                      24.60                                              Carbon Black A                                                                         153.25                                                                              130.00                                                         Carbon Black B       42    87.10 113.40                                       Pigment A                                                                              19.16                                                                Pigment B                  33.90                                              Pigment C            64.52                                                    ZnO      4.94  5.00  5.00  4.10  4.70                                         Oil A    97.03 77.00 58.06                                                    Oil B                            14.20                                        Oil C                      1.30                                               Oil D                      35.20                                              Stearic Acid                                                                           0     0.50  0.50  0.70  1.00                                         Anti-oxidant A       1.50                                                     Anti-oxidant B             0.4                                                Anti-oxidant C                   1.00                                         Anti-oxidant D             2.00                                               Anti-oxidant E             2.00                                               Anti-oxidant F             2.00                                               Wax A                      2.00                                               Chem B                     4.50                                               Accelerator A                                                                          0.743             0.70                                               Accelerator B                                                                          1.073 2.50  2.50                                                     Accelerator C  0.80  0.80                                                     Accelerator D  0.80  0.80                                                     Accelerator E                                                                          1.463 2.00  2.00                                                     Accelerator F                                                                          2.965                                                                Accelerator G                    1.50                                         Accelerator H              1.70                                               Curative A                       0.30                                         Curative B                                                                             0.513             2.70  2.20                                         __________________________________________________________________________

Upon running the recipes through each test, the test results includedthe following:

1. Traditional stress/strain mechanical properties. This measured theoverall quality of mixing process and distributive uniformity.

2. Thermal gravimetric analysis. This measured mass percent, andvariance of major recipe components, that is polymer, oil, carbon blackand mineral fillers.

3. The Monsanto oscillating disc rheometer. This measured the chemicalkinetics of vulcanization chemistry and dynamic shear modulus.

4. Capillary rheology. This evaluated the degree of polymer blending anddispersive mixing by measuring shear stress and viscosity as a functionof shear rate and temperature.

5. Dynamic torque modulus. This measured the degree of dispersivemixing.

6. Transmission electron microscopy. This provided visual evaluation offiller dispersion.

All of the testing in this and the following examples were made with theTable III recipes and were evaluated relative to a statisticallyappropriate batch process mixed control of the identical recipe.

The process of the present invention was carried out in these testsutilizing a co-rotating twin screw device of Berstorff andWerner-Pfleiderer types. For this Example II, the process utilized a twomixing zone approach, wherein the polymers, reinforcement agents andprocessing aids were all admixed together in the first zone, and thevulcanizing agents were then admixed in the second zone. While good toexcellent dispersion of the reinforcing fillers was accomplished,process temperatures were unacceptably high with unacceptable productionrates. Using recipes 1 and 3, process exit temperatures of 160°-200° C.were measured, and premature vulcanization and polymer degradation wasobserved at production rates of approximately 310 kg/s/m³. In thisinstance, the mixing extruder length to diameter ratio ranged from 12:1to 20:1 with residence times of 45-130 seconds.

EXAMPLE III

Analysis of the data suggested from the thermodynamices of the ExampleII, indicated that the two zone mixing approach was incorrect. In thisinstance, a three zone mixing process was utilized wherein the firstmixing zone included the addition of the polymeric materials andapproximately 30% of the reinforcement material such as carbon black andzinc oxide. The second zone added the remainder of the reinforcementmaterial and the processing aids, and the third mixing zone added thevulcanizing agents. Recipes 1, 2 and 3 were mixed at production rates of610 kg/s/m³. The oil, which was the processing aid, was temperatureconditioned at 20° C. The revised material sequence of this Example IIIand the controlled oil addition temperature provided sufficient coolingto reduce the exit temperature to 140°-150° C. The added materialaddition zone extended the length to diameter ratio to 42.5:1. Residencetime of the materials within the extruder was approximately 125 seconds,with a total energy applied ranging from 5.4×10⁵ -6.5×10⁵ J/kg. Good toexcellent carbon black dispersion, comparable to a batch processcontrol, was measured from this Example III using dynamic modulus at 1%and 25% strain as the measure.

While carbon black dispersion appeared to be equal to or improverelative to the batch process, the three zone process implemented inthis Example III continued to produce unacceptable process exittemperatures relative to production rate and high input energy valuesbecause of the carbon black addition to the first zone. Moreover,mineral filler dispersion appeared to be somewhat poorer in this ExampleIII for the continuous mixed material as compared to batch processingmaterial.

Coolant hose products were manufactured from the materials mixed in thisExample III and placed on long-term field trials. After 18 months offield trial, there were no reported product failures. The continuouslymixed materials of recipes 1, 2 and 3, extruded with lower powerrequirements, lower temperatures, and improved surface uniformity whencompared to batch process materials of the same recipes. Analysis of thematerials in this Example III indicated that while improvements inprocessing temperatures and material quality had been made in acontinuous process verses batch process, productivity remained low.There appeared to be some additional productivity potential in theconfiguration before reaching process limits of temperature and/or powerrequirements.

EXAMPLE IV

Yet another set of trials was planned with the same three zoneconfiguration of Example III and material addition schedule but with nomodifications to the process thermodynamics, which therefore focusedmore shear stress to the first mixing zone. This Example IV was set upto test maximum productivity of the three-zone process of the presentinvention. Production rates were elevated from 610 kg/s/m³ to 1,210kg/s/m³ before upper input power and temperature limits were realized.In this Example IV, productivity was doubled and measures of carbonblack and mineral filler dispersion were substantially improved.

Unfortunately, similar temperature and pressure data was not collectedin Examples II and III, so clear comparisons could not be made. It wasexpected, however, that the total exposure to polymer degradingtemperatures was less in this Example IV configuration than in theconfigurations previously employed.

One significant liability associated with sequential addition ofmaterials in a continuous process is the consistent mass flow ofindividual raw material streams. Any continuous processing system isprimarily a first in, first out system with only modest back blendingalong the axis of material flow (22). Non-uniformity of mass flows ofthe separate ingredient streams can result in unacceptable constituentvariability in the final product. Analysis for percent of polymer,carbon black, oil and mineral fillers in the results of Example IIIindicated unacceptable levels of variation. After obtaining productionrates approaching desirable commercial levels in this Example IV,analysis of variation was made, and examination of the data in thisparticular Example IV indicated that the continuously mixed recipe 3 wasuniformly more consistent than comparable batch process mixed material.

EXAMPLE V

Another set of trials, this time utilizing recipes 1 and 3, wasinitiated in which the thermodynamics of the process were furtherdifferentiated into the four mixing zone configuration outlined in FIGS.1 and 2 and described above. In the four zone configuration in thisparticular Example V the polymers, zinc oxide and anti-oxidants wereadded in the first zone 12. In the second zone 14, the carbon blacks andoils to approximately 90% of the volume of the mixture from the firstzone 12 were added. In the third zone 16, the remainder of the carbonblack and mineral fillers and oils were added. Finally, thevulcanization agents were added to the fourth mixing zone 18. This wasas described previously. The thermodynamic objective of this Example Vwas to completely isolate the high shear, high energy input portion ofthe process to the polymeric materials in the first mixing zone 12. Therationale was to masticate the polymers at a high rate of energy inputwithin only the first mixing zone 12, elevate their temperatures abovenormal processing temperatures so as to reduce their viscosities to verylow values prior to introduction of the reinforcing fillers at thebeginning the second mixing zone 14. This process would, necessarily,require very short, that is 15-20 seconds, residence times to avoidthermal degradation of the polymers.

The effect of this Example V was to apply the energy necessary toachieve good mixing rheology, that is low viscosity, only to thematerial components which are susceptible to shearing energy. The storedthermal energy, temperature, was present in a minor percentage of thetotal recipe mass. The addition of the carbon black and oil in thesecond and third zones 14 and 16 were then easily disbursed into the lowviscosity polymer volume and served to absorb the energy present in thepolymer, thus reducing the temperature of the mixture to an acceptableprocessing level. The addition temperature of the reinforcing fillerswas room temperature, that is 23° C., and the oil was temperaturecontrolled to about 20° C. In order to maintain a more constant workingvolume-to-gross volume ratio, the gross volumes of the second, third andfourth zones 14, 16 and 18, respectively, were increased with respect tothe first zone 12.

The vulcanizing agents were added to the fourth zone 18 to isolate thechemical reactivity occurring during curing from the high temperaturesand residence times present earlier in the process of the invention,thereby preventing premature vulcanization.

An important feature of this Example V was the ability to manipulate thefirst zone 12 residence time, exit temperature and exit viscosity bymeans of adjustable clearance capability at the exit of the first zone12. This feature facilitated a transfer of thermodynamic work from thesecond and third zones to the first zone. When the exit clearance wasreduced, thereby transferring more of the work to the first zone 12,productivity was increased by approximately 20%, and an unexpectedreduction in applied power, in the range of 3.6×10⁵ J/kg to 4.5×10⁵ J/kgwas measured. Temperatures and pressures remained within acceptableprocess levels.

Analysis of the results of this Example V indicated consistentlyimproved uniformity of material properties. The traditionalstress/strain mechanical properties for recipe 1 mixed in this Example Vindicated similar good compliance with the established specification anduniformity measures which are substantially better than the batchprocess standards. As a result, it can be seen from Example V that thepreferred four mixing zone configuration as illustrated in FIGS. 1 and 2provided substantially improved results as compared to batch processingof the same recipes.

As can be seen from the above, the present invention provides aneconomic means of producing relatively improved homogeneity of finalmaterial properties of elastomeric compositions. Experimental resultsindicate an improvement of at least 50% in standard deviation of finalmaterial property when compared to traditional batch mixing. Microuniformity of material distribution was even better on the basis of verysmall samples. Fine dispersion of reinforcing fillers was relativelyimproved by 5-20% when compared to batch mixed materials of the sameformulation. Viscosity of the elastomeric composition produced with thepresent invention was much lower and consistently more uniform, atextrusion and calendaring temperatures resulting in dimensionally moreconsistent rubber components. In formulations using discontinuous shortfiber reinforcement, fiber incorporation and dispersion wassubstantially easier and better when compared to batch mixed processes.The present invention, therefore, affords the opportunity to produce newand unique polymer blends and/or alloys with thermoplastic polymerswhich are thermodynamically impossible to control when using traditionalbatch process mixers. The independent/staged mixing process of thepresent invention not only provides a more uniform elastomericcomposition product, but also provides a much shorter period of time toachieve the same inasmuch as it only requires one pass through a deviceincorporating the process of the present invention as compared to aplurality of passes using the batch mixing process. Thus, a more uniformproduct can be produced in less time and utilizing less energy, therebyproviding substantial economic savings as compared to existingtechnology.

The foregoing description and the illustrative embodiments of thepresent invention have been described in detail in varying modificationsand alternate embodiments. It should be understood, however, that theforegoing description of the invention is exemplary only, and that thescope of the invention is be limited only to the claims as interpretedin view of the prior art. Moreover, the invention illustrativelydisclosed herein, suitably may be practiced in the absence of anyelement which is not specifically disclosed herein.

The embodiments of the invention in which an exclusive property or privilege is claimed are defined as follows:
 1. In a process for producing elastomeric compositions by mixing an elastomeric material, a reinforcing agent, a processing aid and a vulcanizing agent, the improvement comprising the successive steps of:simultaneously shearing, heating to a temperature of a first operating temperature range, and sufficiently reducing the viscosity of the elastomeric material to facilitate admixing at least a portion of the reinforcing agent; adding at least a portion of the reinforcing agent having a lower temperature than that temperature of the first operating temperature range of the so heated and reduced viscosity elastomeric material; and admixing the lower temperature reinforcing agent to the so heated and reduced viscosity elastomeric material while simultaneously 1) cooling the elastomeric material by means of the lower temperature reinforcing agent, and 2) forming a mixture of elastomeric material and reinforcing agent having a temperature that is less than the temperature of the so heated elastomeric material.
 2. The process of claim 1 and further including after the step of admixing, the steps, of separately adding and admixing at least a portion of the processing aid having a temperature less than that temperature of the so heated elastomeric material, and aiding cooling of the higher temperature elastomeric material and forming a mixture of elastomeric material, reinforcing agent and processing aid having a temperature of a second operating temperature range that is less than the so heated temperature of the elastomeric material.
 3. The process of claim 1 and further including the successive steps of separately adding and admixing the vulcanizing agent therewith and forming a mixture of elastomeric material, reinforcing agent, processing aid and vulcanizing agent having a temperature of a third operating temperature range.
 4. The process of claim 2 and further including the successive steps of:separately adding and admixing a second portion of reinforcing agent having a temperature less than that temperature of the mixture of elastomeric material, reinforcing agent and processing aid, and separately adding and admixing a second portion of the processing aid having a temperature less than that temperature of the heated elastomeric material.
 5. The process of claim 3 and further including the successive steps of expelling the mixture as an elastomeric composite.
 6. The improvement as claimed in claim 3 wherein said first operating temperature range is approximately 130°-220° C., said second operating temperature range is approximately 110°-160° C., and said third operating temperature range is approximately 115°-150° C.
 7. The improvement as claimed in claim 3 wherein a gross energy applied to process steps in achieving the temperature of the first operating temperature range comprises approximately 5.4×10⁵ to 1.1×10⁶ J/kg, a gross energy applied to process steps associated in achieving the temperature of the second operating temperature range comprises approximately 4.3 to 7.2×10⁴ J/kg, and a gross energy applied to process steps associated in achieving the temperature of the third operating temperature range comprises approximately 3.6×10⁴ to 1.1×10⁵ J/kg.
 8. The improvement as claimed in claim 1 comprising limiting shearing and preventing depolymerization of said polymeric material.
 9. The improvement as claimed in claim 3 wherein a volume percentage of said mixture is maintained substantially the same throughout the processing steps.
 10. The improvement as claimed in claim 3 wherein prior to the step of shearing, the step of admixing up to thirty percent by weight of the reinforcing agent with the elastomer and maintaining said first operating temperature range at approximately 130°-220° C., said second operating temperature range at approximately 110°-160° C., and said third operating temperature range at approximately 115°-150° C.
 11. The improvement as claimed in claim 3 wherein during or prior to the shearing, heating and reducing steps, the step of adding a polymer which is different than the elastomeric material.
 12. A process for producing elastomeric compositions utilizing an elongate twin-screw extruder, said process comprising:admixing components of a composition including elastomeric material, a reinforcing agent, a processing aid and a vulcanizing agent in sequential staged-additions along a length of said extruder which has at least five successively interconnected mixing zones and comprising the steps of: adding and mixing said elastomeric material along the first mixing zone of the extruder and simultaneously shearing, heating and sufficiently reducing the viscosity of the elastomeric material along the first mixing zone of the extruder to facilitate admixing at least a portion of the reinforcing agent; separately and sequentially adding at least a portion of a cooler reinforcing agent and processing aid to the so heated elastomeric along the second mixing zone of the extruder while simultaneously cooling the elastomeric material with said reinforcing agent and processing aid; separately and sequentially adding a second portion of a cooler reinforcing agent and processing aid to a local component mixture along the third mixing zone of the extruder while cooling the component mixture with a second portion of reinforcing agent and processing aid; adding and admixing the vulcanizing agent to a local-component mixture along the fourth mixing zone of the extruder; and moving a local component mixture along and through the fifth zone of the extruder and extruding said mixture in the form of said elastomeric composition.
 13. The process as claimed in claim 12, wherein said material is moved along said extruder having a length to diameter ratio of approximately 50-55 to
 1. 14. The process as claimed in claim 12, wherein said mixture is admixed in said first mixing zone under high shear conditions.
 15. The process as claimed in claim 12, wherein polymeric material is added in a coarsely chopped condition.
 16. The process as claimed in claim 12, wherein said mixing zones are maintained in a substantially starved condition.
 17. The process as claimed in claim 16, wherein said component mixture is maintained at substantially 15-30% of the volume of each said mixing zone in order to facilitate relative uniform energy flux, volume blending and residence time in each said mixing zone.
 18. The process as claimed in claim 12, wherein the productivity rate of said process is up to 2,500 kg/sec.m³.
 19. The process as claimed in claim 12, wherein the energy balance of said extruder is at steady state during operation of said process. 